PharmD Jobs at Eli Lilly | Apply Now For The Clinical Surveillance Scientist Role
Eli Lilly is seeking a Clinical Surveillance Scientist in Bangalore, Karnataka, to join its Global Patient Safety (GPS) organization. This role is vital to advancing pharmacovigilance by detecting safety signals, evaluating safety risks, responding to regulatory inquiries, and driving scientific excellence across drug development and marketed products. If you’re passionate about drug safety and clinical research, this opportunity allows you to make a global impact.
- Job Position: Clinical Surveillance Scientist
- Location: Bangalore, Karnataka, India
- Job ID: R-89283
About the Company
At Eli Lilly, we combine caring with discovery to improve lives around the globe. Headquartered in Indianapolis, Indiana, Lilly is a leader in healthcare innovation, bringing life-changing medicines to patients while supporting communities through volunteerism and philanthropy.
Job Description
The Clinical Surveillance Scientist is a key member of the Global Patient Safety (GPS) organization. This position provides scientific, clinical, and pharmacovigilance expertise to support Lilly’s pipeline and marketed medicines. The role involves leading safety signal detection, evaluating safety data, performing risk assessments, supporting regulatory inquiries, and authoring safety reports to ensure compliance with global regulations.
Key Responsibilities
Signal Detection & Safety Evaluation
- Lead identification and evaluation of safety signals from internal and external data sources.
- Develop and review label changes in collaboration with regulatory and medical teams.
- Lead safety team meetings for clinical and marketed products.
- Define strategies for collecting, analyzing, and reporting safety data.
- Collaborate with physicians, scientists, and pharmacoepidemiologists to ensure comprehensive safety evaluations.
- Communicate safety findings to internal and external stakeholders.
Risk Assessment & Regulatory Support
- Author safety sections of global regulatory reports such as DSURs, PSURs, PADERs, PBRERs, and Risk Management Plans.
- Provide input to labeling updates, HCP communications, and regulatory responses.
- Ensure compliance with international pharmacovigilance requirements.
Leadership & Collaboration
- Mentor and coach junior scientists in patient safety.
- Drive process improvements and innovative approaches in pharmacovigilance.
- Collaborate across functional teams to strengthen safety practices.
- Represent Lilly in interactions with regulatory authorities (FDA, EMA, MHRA, etc.).
Qualifications
Minimum Requirements
- Advanced medical-related graduate degree (PharmD, PhD, or advanced nursing/clinical specialty) with 1–3 years’ relevant scientific experience; OR
- BS in health/scientific field with 7–10 years of pharma industry or clinical trial experience; OR
- 3–5 years of clinical or pharmaceutical experience with at least 2 years in clinical development.
Preferred Skills
- Strong clinical knowledge across disease states, pharmacology, and drug safety.
- Experience in Global Patient Safety or pharmacovigilance.
- Ability to manage multiple deliverables effectively.
- Strong communication and cross-functional collaboration skills.
Keywords: Clinical Surveillance Scientist jobs, Job Postings, pharmacovigilance jobs Bangalore, drug safety jobs Eli Lilly, PharmD Jobs at Eli Lilly, research and development careers India, clinical research jobs Bangalore
